可待因给药对成年Wistar大鼠前额皮质和小脑的免疫组化研究

V. Archibong, T. Ekanem, A. Igiri, Ann Monima Lemuel, I. Usman, A. Okesina, N. J. Obosi
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引用次数: 7

摘要

尽管处方阿片类药物的使用增加带来了危险,但关于处方阿片类药物对大脑的具体影响的研究有限。本研究的目的是评估可待因药物对Wistar大鼠前额皮质和小脑的影响。本研究使用的药物为ArchilinTM含可待因糖浆和二氢可待因30 mg片剂。雄性Wistar大鼠30只,分为A、B、C、D、E 5组,n = 6。A组作为对照组,给予生理盐水,B组给予1 mg/kg体重双氢可待因治疗,C组给予2 mg/kg体重双氢可待因治疗,D组给予2 ml/kg体重ArchilinTM加可待因糖浆治疗,E组给予4 ml/kg体重ArchilinTM加可待因糖浆治疗。口服和每日给药21天。在治疗期结束时,通过腹腔注射盐酸氯胺酮处死动物,在收获前脑内灌注磷酸盐缓冲盐水和正规盐水,并在10%中性缓冲福尔马林中固定。获得前额皮质和小脑切片,并使用GFAP染色进行免疫组织化学研究。研究结果表明,长期服用可待因药物在治疗组的前额叶皮层和小脑中产生炎症反应。这种神经炎症反应是一种病理过程的指示,可导致神经元变性、胶质变性和前额叶皮层和小脑的生理过程改变。
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Immunohistochemical studies of codeine medication on the prefrontal cortex and cerebellum of adult Wistar rats
Abstract Despite the dangers associated with the increased use of prescription opioid drugs, limited researches have addressed the specific effects of prescription opioids on the brain. The objective of this study was to assess the effects of codeine medication on the prefrontal cortex and cerebellum of Wistar rats. The drugs, ArchilinTM with codeine syrup and Dihydrocodeine 30 mg tablets were used for this study. Thirty (30) male Wistar rats were divided into 5 groups labeled A, B, C, D, and E, n = 6. Group A served as control and was given normal saline, group B was treated with 1 mg/kg bodyweight dihydrocodeine, group C was treated with 2 mg/kg bodyweight dihydrocodeine, group D was treated with 2 ml/kg bodyweight ArchilinTM with codeine syrup and group E was treated with 4 ml/kg bodyweight ArchilinTM with codeine syrup. Drugs were administered orally and daily for 21 days. At the end of the treatment period, animals were sacrificed via intraperitoneal injection of ketamine hydrochloride, brains were perfused with phosphate-buffered saline and formal saline before harvested and postfixed in 10% neutral buffered formalin. Sections of the prefrontal cortex and cerebellum were obtained and processed for immunohistochemical studies using GFAP stain. Results from the study suggested that prolonged administration of codeine medication produced an inflammatory reaction in the prefrontal cortex and cerebellum of treatment groups. This neuroinflammatory reaction is an indicator of a pathologic process that could lead to neuronal degeneration, glial degeneration, and altered physiologic process in the prefrontal cortex and cerebellum.
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